TY - JOUR
T1 - Polymyalgia rheumatica during combination therapy with atezolizumab plus bevacizumab for advanced hepatocellular carcinoma
AU - Dosoden, Naoki
AU - Kuzuya, Teiji
AU - Ito, Yumi
AU - Nishino, Jo
AU - Ohno, Eizaburo
AU - Kawabe, Naoto
AU - Hashimoto, Senju
AU - Hirooka, Yoshiki
AU - Yasuoka, Hidekata
N1 - Publisher Copyright:
© 2023, Japanese Society of Gastroenterology.
PY - 2023/8
Y1 - 2023/8
N2 - The combination therapy of atezolizumab, an anti-programmed cell death ligand-1 antibody, plus bevacizumab (Atz/Bev) is widely used to treat patients with advanced hepatocellular carcinoma (HCC). The development of polymyalgia rheumatica (PMR) during immune checkpoint inhibitor therapy for patients with HCC has not been reported to date. Two patients who developed PMR during Atz/Bev therapy for advanced HCC are reported. Both patients developed fever, bilateral symmetrical shoulder pain, morning stiffness, and an elevated C-reactive protein level. Their symptoms improved rapidly with prednisolone (PSL) 15–20 mg/d, and their C-reactive protein levels decreased. In PMR, long-term low-dose PSL should be administered. In the present patients who developed PMR as immune-related adverse events, starting with a small dose of PSL resulted in rapid improvement of symptoms.
AB - The combination therapy of atezolizumab, an anti-programmed cell death ligand-1 antibody, plus bevacizumab (Atz/Bev) is widely used to treat patients with advanced hepatocellular carcinoma (HCC). The development of polymyalgia rheumatica (PMR) during immune checkpoint inhibitor therapy for patients with HCC has not been reported to date. Two patients who developed PMR during Atz/Bev therapy for advanced HCC are reported. Both patients developed fever, bilateral symmetrical shoulder pain, morning stiffness, and an elevated C-reactive protein level. Their symptoms improved rapidly with prednisolone (PSL) 15–20 mg/d, and their C-reactive protein levels decreased. In PMR, long-term low-dose PSL should be administered. In the present patients who developed PMR as immune-related adverse events, starting with a small dose of PSL resulted in rapid improvement of symptoms.
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U2 - 10.1007/s12328-023-01800-2
DO - 10.1007/s12328-023-01800-2
M3 - Article
C2 - 37071371
AN - SCOPUS:85152966908
SN - 1865-7257
VL - 16
SP - 567
EP - 571
JO - Clinical Journal of Gastroenterology
JF - Clinical Journal of Gastroenterology
IS - 4
ER -